Dr Kids Pain and Fever

Dr Kids Pain and Fever is an FDA-registered drug product whose active ingredient is ACETAMINOPHEN. It is labelled by CalmCo LLC taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 73282-2522, application M012, label effective 20260706. It is one of 274 FDA drug label records sharing the active ingredient ACETAMINOPHEN. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing ACETAMINOPHEN are most often described in connection with: temporary relief, minor aches, pains due, sore throat, reduce fever. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses For the temporary relief of minor aches and pains due to sore throat headache and to reduce fever

Directions this product does not contain directions or complete warnings for adult use do not exceed 5 doses in a 24-hour period (see liver warning) follow the “Easy to Use” instructions on the pouch corresponds to your child’s age use the dose that Age (Years) Dose* under 2 consult a doctor 2 to under 6 1 vial (5 mL) 6 to 11 2 vials (10 mL) *dose may be repeated every 4 hours while symptoms persist, up to five times a day or as directed by a doctor.

Warnings Liver warning: This product contains acetaminophen. Severe liver damage may occur if your child takes more than 5 doses in 24 hours, which is the maximum daily amount for this product acetaminophen Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include: skin redness blisters rash Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly Do not use with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist Ask a doctor before use if your child has liver disease Ask a doctor or pharmacist before use if your child is taking the blood thinning drug warfarin Stop use and ask a doctor if pain gets worse or lasts more than 5 days fever gets worse or lasts more than 3 days edness or swelling is present any new symptoms appear Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Prompt medical attention is critical even if you do not notice any signs or symptoms.

FDA lists 274 drug label records with ACETAMINOPHEN as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is Dr Kids Pain and Fever used for?
Uses For the temporary relief of minor aches and pains due to sore throat headache and to reduce fever

Who makes Dr Kids Pain and Fever?
CalmCo LLC is the labeler of record for Dr Kids Pain and Fever. 274 FDA label records share the active ingredient ACETAMINOPHEN, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Dr Kids Pain and Fever come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Dr Kids Pain and Fever prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing ACETAMINOPHEN?
Yes. 274 FDA drug label records list ACETAMINOPHEN as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Dr Kids Pain and Fever been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.